SANITAXE

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO LTD
Effective date
2014-07-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:35:35

Label at a glance#

ProductSANITAXE
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. when water, soap and towel are not available. recommended for repeated use.

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62%

PURPOSE

INDICATIONS & USAGE SECTION

Antiseptic

USES

OTC - PURPOSE SECTION

hand sanitizer to help decrease bacteria on the skin. when water, soap and towel are not available. recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and or flame. Do not apply around eyes. Do not use in ears and mouth. When using this product, avoid contact with eyes. In case of contact, flush eyes with water. Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76176-003-082020-01-31C16284748780-19d75b9d1-2334-f424-e053-dadaa90a57ce757a3c0d-ae40-4a48-b6a3-0600d50c7d96

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-00376176-003-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
582ae543-a5f2-4fad-9cee-765ef78d507a757a3c0d-ae40-4a48-b6a3-0600d50c7d962014-07-31WarningsExact identifier
spl id: 582ae543-a5f2-4fad-9cee-765ef78d507a
spl set id: 757a3c0d-ae40-4a48-b6a3-0600d50c7d96

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.